nsv6897864
- Organism: Homo sapiens
- Study:nstd229 (Jun et al. 2023)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh38
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:94,119
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 232 SVs from 47 studies. See in: genome view
Overlapping variant regions from other studies: 232 SVs from 47 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nsv6897864 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000010.11 | Chr10 | 30,839,815 | 30,933,933 | ||
nsv6897864 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000010.10 | Chr10 | 31,128,744 | 31,222,862 |
Variant Call Information
Variant Call ID | Type | Method | Analysis |
---|---|---|---|
nssv18580516 | duplication | Sequencing | Split read and paired-end mapping |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
---|---|---|---|---|---|---|---|---|---|
nssv18580516 | Submitted genomic | NC_000010.11:g.308 39815_30933933dup | GRCh38 (hg38) | NC_000010.11 | Chr10 | 30,839,815 | 30,933,933 | ||
nssv18580516 | Remapped | Perfect | NC_000010.10:g.311 28744_31222862dup | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 31,128,744 | 31,222,862 |
No validation data were submitted for this variant
No clinical assertion data were submitted for this variant
Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.
Genotype Information
Variant Call ID | Allele Frequency (AF) | Allele Count (AC) | Allele Number (AN) |
---|---|---|---|
nssv18580516 | 2.8e-05 | 8 | 275756 |